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Aesculap JF217R

by Aesculap, Inc.

Part of a family of 95 devices: see the family page

Ref JF217R

Aesculap JF217R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 7 Jul 2025 (Basic UDI-DI 4039239000000402ZL) and listed in FDA GUDID since 8 May 2020 (UDI-DI 04038653128082), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000402ZL Basic UDI-DI 04038653128082UDI-DIDate7 Jul 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653128082 UDI-DI Date8 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000000402ZL registered 7 Jul 2025 Active
  • FDA GUDID UDI-DI 04038653128082 listed 8 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653128082
  2. Registered EUDAMED 4039239000000402ZL

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Aesculap
Generic name
Surgical instrument/implant rack
Device name
Sterilization tray
Model / Ref / Catalog
JF217R
Primary DI / UDI-DI
04038653128082
Basic UDI-DI
4039239000000402ZL
Direct marketing DI
04038653128082
FDA product code
FSM
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
GMDN term
Surgical instrument/implant rack
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical instrument/implant rack

Similar devices in this category

Other devices filed under TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

  • Sterilise before use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)